Dentifrice compositions comprising an abrasive system and a surfactant system

Abstract

compositions comprising, in an aqueous vehicle, an abrasive system containing an alkali metal bicarbonate and a surfactant system, where the surfactant system comprises a non-ionic poly(hydroxypropyl ether) surfactant. Such compositions are particularly useful as oral hygiene compositions.

These compositions may be used as, or for the manufacture of, a dentifrice in the form of a paste, a gel, a liquid or a chewing gum.

Description

The present invention relates to new compositions comprising, in an aqueous vehicle, an abrasive system containing at least one alkali metal bicarbonate and a surfactant system containing at least one non-ionic poly(hydroxypropyl ether) surfactant, these compositions being represented in particular by compositions for oral hygiene.

The invention also relates to the use of these compositions as, or for manufacture of, a dentifrice in the form of a paste, a gel, a liquid or a chewing gum.

Use is commonly made, in the field of oral hygiene, of alkali metal bicarbonates, in particular for neutralizing the acids responsible for caries and especially for their abrasiveness.

Moreover, in order to formulate so-called "aqueous" dentifrices, thus described because they contain at least 3% by weight of water, use has until now been made of surface-active agents of anionic type, the role of which is to introduce both a satisfactory foaming power and a satisfactory detergent power. Mention may more particularly be made, among the latter, of sodium lauryl sulphate, which is indeed the most commonly employed.

Now, the inventors have observed that, in these formulations, the alkali metal bicarbonates, initially introduced in the form of solid particles (powders), are partially dissolved. This partial dissolution brings about a significant loss in the abrasive power associated with the final composition. In order to overcome this disadvantage, the inventors have carried out a great deal of research into the matter and have discovered, surprisingly, that a much lower solubilization of the alkali metal bicarbonate could be obtained in aqueous compositions comprising a non-ionic surfactant system of the poly(hydroxypropyl ether) type, compared to the degree of solubilization in aqueous compositions comprising a sodium lauryl sulphate.

Thus, using equal amounts of bicarbonates, the abrasive power of the compositions in accordance with the invention is markedly greater than that of the compositions of the prior art. In addition, the surfactant system selected according to the invention has an excellent foaming and detergent power.

These discoveries are the basis of the present invention.

The subject of the present invention is therefore new compositions of the type comprising, in an aqueous vehicle, an abrasive system containing at least one alkali metal bicarbonate and a surfactant system, which are characterized in that the said surfactant system comprises at least one non-ionic poly(hydroxypropyl ether) surfactant.

Another subject of the present invention is compositions of this type for oral use, in particular dentifrices.

The present invention is also targeted at the use of these compositions as, or for the manufacture of, a dentifrice which can be in the form of a paste, a gel, a liquid or a chewing gum.

However, other characteristics, aspects, subjects and advantages of the invention will become still more clearly apparent on reading the description and the examples which follow.

The alkali metal bicarbonate which can be used according to the invention is preferably chosen from sodium bicarbonate or potassium bicarbonate.

The surfactants of poly(hydroxypropyl ether) type are products which are already known per se. Preferably, according to the present invention, the non-ionic poly(hydroxypropyl ether) surfactant(s) are chosen from the compounds of following structures:

(A) The compounds corresponding to the formula (I): ##STR1## in which the C₃ H₅ (OH)O group is identical or different and represents the following structures (I.a), (I.b) and (I.c): ##STR2## and R and n have, together, one of the meanings a), b), or c) below: a) R denotes a C₁0 -C₁4 alkyl radical or a mixture of C₁0 -C₁4 alkyl radicals, and n is a whole or decimal number varying from 2 to 10 and preferably from 3 to 6,

b) R denotes a group of formula (II):

R₂ --CONH--CH₂ --CH₂ --O--CH₂ --CH₂ --(II),

in which R₂ denotes a C₁1 -C₁7 -alkyl or -alkenyl radical or a mixture of C₁1 -C₁7 -alkyl and/or -alkenyl radicals, and n denotes a whole or decimal number varying from 1 to 5 and preferably from 1.5 to 4,

c) R denotes a group of formula (III):

R₃ --CHOH--CH₂ -- (III),

in which R₃ denotes a C₇ -C₂1 -aliphatic, -cycloaliphatic or -arylaliphatic radical, or a mixture thereof, the aliphatic chains denoting in particular alkyl chains which can contain from 1 to 6 ether, thioether and/or hydroxymethylene groups, and n denotes a whole or decimal number varying from 1 to 10.

These surfactants of formula (I) can be prepared according to the processes described in French patent documents 1,477,048, 2,328,763 and 2,091,516, the disclosures of which are hereby incorporated by reference.

(B) The non-ionic poly(hydroxypropyl ether) compounds prepared by condensation, in acid catalysis, and at a temperature ranging from 50° to 120°C, of 2 to 10 mol, preferably, 2.5 to 6 mol, of glycidol per mole of alcohol containing 10 to 14 carbon atoms or of alpha-diol containing 10 to 14 carbon atoms, the glycidol being slowly added to the alcohol or to the alpha-diol.

The process for the preparation of these compounds is described in French patent document 2,169,787, the disclosure of which is hereby incorporated by reference.

(C) The non-ionic poly(hydroxypropyl ether) compounds prepared by polyaddition of glycerol monochlorohydrin to a polyhydroxylated organic compound in the presence of a strong base, with removal of the water, by distillation, as it is formed. A base is considered strong at a pH greater than 10.

These compounds are described in French patent document 2,574,786, the disclosure of which is hereby incorporated by reference.

The more particularly preferred compounds according to the invention, among the non-ionic poly(hydroxypropyl ether) surfactants described in paragraphs (A), (B) and (C) above, are:

i) those of following formulae (IV) and (V): ##STR3## in which formula (V) R₁ denotes a mixture of C₁0 H₂1 and C₁2 H₂5 alkyl radicals,

2i) the non-ionic poly(hydroxypropyl ether) compounds prepared by condensation, in alkaline catalysis, of 3.5 mol of glycidol with an alpha-diol having 12 carbon atoms, according to the process described in French Patent FR 2,091,516,

3i) the compounds of formula (VI):

R₂ --CONH--CH₂ --CH₂ --O--CH₂ --CH₂ --O--(--CH₂ --CHOH--CH₂ --O--)₃.5 --H (VI)

in which R₂ denotes a mixture of radicals comprising the following alkyl and alkenyl radicals: C₁1 H₂3, C₁3 H₂7, the radicals derived from coconut fatty acids and the radical derived from oleic acid,

4i) the compounds prepared by condensation of 3.5 mol of glycidol with a mixture of C₁1 -C₁4 alpha-diols described in French patent document 2,091,516.

Dodecanediol polyglycerolated with 3.5 mol of glycerol is more particularly preferred.

According to a preferred embodiment of the compositions according to the invention, the surfactant system contains only non-ionic surfactant(s) in accordance with the invention.

In the compositions according to the invention, the at least one alkali metal bicarbonate is generally present in concentrations by weight of from approximately 0.5 to 80% and preferably from approximately 1 to 50%, and the at least one non-ionic poly(hydroxypropyl ether) surfactant is generally present in concentrations by weight of from approximately 0.1 to 10% and preferably from approximately 0.2 to 5% with respect to the total weight of the composition.

The compositions in accordance with the invention which are intended for oral hygiene can contain, in addition to the alkali metal bicarbonate and the non-ionic poly(hydroxypropyl ether) surfactant, either as a vehicle or for their own activity, excipients or ingredients commonly used in products for oral use.

The compositions in accordance with the invention are prepared according to the usual processes corresponding to the vehicles chosen. The physiologically acceptable vehicle can be different in nature according to the form chosen for the composition: optionally thickened aqueous or aqueous/alcoholic medium, pasty or solid excipient, gum, and the like.

Depending upon the desired forms, these compositions can also contain other abrasive agents, among which mention may be made of, for example, silica, alumina, calcium hydrogenphosphate and calcium carbonate, anticarious agents such as, for example, sodium or potassium or amine fluorides or sodium monofluorophosphate, antibacterial agents such as, for example, chlorhexidine, alexidine, hexetidine, cetylpyridinium chloride or 2,4,4'-trichloro-2'-hydroxydiphenyl ether, antiinflamnmatory agents, antihalitosis agents, enzymes, vitamins, trace elements, haemostatic agents, healing agents and agents which are active on the gum. Moreover, they can contain other usual agents such as binding agents, sweeteners, humectants or fresheners, preservatives, dyes, fragrances, flavouring agents, peptizing agents and plasticizers.

Concrete, but in no way limiting, examples illustrating the invention will now be given.

EXAMPLE 1

The preservation of the sodium bicarbonate crystals in aqueous solutions containing 2% of non-ionic poly(hydroxypropyl ether) surfactant and the dissolution of the same crystals in solutions containing 2% of sodium lauryl sulphate were studied, at different concentrations, by direct observation of the said solutions with an optical microscope.

To do this, the six compositions below (% by weight) were prepared and were then brought, with stirring, to a temperature of 40°C, in order to obtain solutions. These solutions were then allowed to return to a temperature of 20°C and they were observed with a microscope.

______________________________________
2%      2%
11%      12%      13%    Non-ionic
Na lauryl
Solution
NaHCO3
NaHCO3
NaHCO3
surfactant*
sulphate
______________________________________
S1     X                        X
S2     X                                X
S3              X               X
S4              X                       X
S5                       X      X
S6                       X              X
______________________________________

dodecanediol polyglycerolated with 3.5 mol of glycerol, prepared according to the process described in French patent document 2,091,516.

The photographs of these observations are attached and labelled FIGS. 1-6. FIGS. 1 to 6 correspond to the photographed solutions 1 to 6 respectively. In these photographs, the crystalline network which appears at the bottom of the solutions S2, S4 and S6 was identified as being a sodium lauryl sulphate network.

BRIEF DESCRIPTION OF THE FIGURES

The file of this patent contains at least one drawing executed in color. Copies of this patent with color drawing(s) will be provided by the Patent and Trademark Office upon request and payment of the necessory fee.

FIG. 1 depicts a microscope view of crystals in solution S1 containing 11% NaHCO₃ in an aqueous solution of 2% nonionic surfactant.

FIG. 2 depicts a microscope view of a sodium lauryl sulphate crystalline network in solution S2 containing 11% NaHCO₃ in an aqueous solution of 2% sodium lauryl sulphate.

FIG. 3 depicts a microscope view of crystals in solution S3 containing 12% NaHCO₃ in an aqueous solution of 2% nonionic surfactant.

FIG. 4 depicts a microscope view of a sodium lauryl sulphate crystalline network in solution S4 containing 12% NaHCO₃ in an aqueous solution of 2% sodium lauryl sulphate.

FIG. 5 depicts a microscope view of crystals in solution S5 containing 13% NaHCO₃ in an aqueous solution of 2% nonionic surfactant.

FIG. 6 depicts a microscope view of a sodium lauryl sulfate crystalline network in solution S6 containing 13% NaHCO₃ in an aqueous solution of 2% sodium lauryl sulphate.

The solutions S5 and S6 were supersaturated with sodium bicarbonate. In both cases, crystals were therefore observed with a microscope. The solution S1 according to the invention exhibited crystals whereas the solution S2, which constituted the prior art, did not.

Likewise, the solution S3 according to the invention exhibited crystals whereas the solution S4, which constituted the prior art, did not.

In conclusion, sodium bicarbonate was dissolved to a lesser extent in non-ionic poly(hydroxypropyl ether) surfactant medium than in sodium lauryl sulphate medium.

EXAMPLE 2

A toothpaste which was made in accordance with the invention is illustrated here.

______________________________________
Sodium bicarbonate, Codex 0/13, sold by the
20 g
company Solvay
Thickening silica, sold under the name "Tixosil 333"
11 g
by the company Rhone-Poulenc
Sodium carboxymethylcellulose, sold under the name
1.3 g
"Blanose 9M31F" by the company Hercules
Sorbitol as an aqueous solution containing 70%
12.6 g AM
of active material (AM)
Dodecanediol polyglycerolated with 3.5 mol of
1.5 g
glycerol
Titanium dioxide         0.5 g
Sodium fluoride          0.33 g
Preservative, sweetener, fragrance
q.s.
Water                    q.s. for 100 g
______________________________________

Claims

1. A composition comprising, in an aqueous vehicle, an abrasive system containing at least one alkali metal bicarbonate and a surfactant system, wherein said surfactant system comprises at least one nonionic poly(hydroxypropyl ether) surfactant.

2. A composition according to claim 1, wherein said aqueous vehicle is a physiologically acceptable vehicle containing at least 3% by weight of water with respect to the total weight of the composition.

3. A composition according to claim 1, wherein said at least one alkali metal bicarbonate is sodium bicarbonate or potassium bicarbonate.

4. A composition according to claim 1, wherein said at least one non-ionic poly(hydroxypropyl ether) surfactant is selected from the following compounds:

(A) The compounds corresponding to the formula (I): ##STR4## in which the C₃ H₅ (OH)O group is identical or different and represents the following structures (I.a), (I.b), and (I.c): ##STR5## and R and n have, together, one of the meanings a), b), or c) below: a) R denotes a C₁0 -C₁4 alkyl radical or a mixture of C₁0 -C₁4 alkyl radicals, and n is a whole or decimal number from 2 to 10,

b) R denotes a group of formula (II):

R₂ --CONH--CH₂ --CH₂ --O--CH₂ --CH₂ --(II),

in which R₂ denotes a C₁1 -C₁7 -alkyl or -alkenyl radical, a mixture of C₁1 -C₁7 -alkyl radicals, a mixture of C₁1 -C₁7 -alkenyl radicals, or a mixture of C₁1 -C₁7 -alkyl radicals and C₁1 -C₁7 -alkenyl radicals, and n denotes a whole or decimal number from 1 to 5,

c) R denotes a group of formula (III):

R₃ --CHOH--CH₂ -- (III),

in which R₃ denotes a C₇ -C₂1 -aliphatic, C₇ -C₂1 -cycloaliphatic or C₇ -C₂1 -arylaliphatic radical, or a mixture of any of said C₇ -C₂1 radicals, and n denotes a whole or decimal number from 1 to 10;

(B) the poly(hydroxypropyl ether) compounds prepared by condensation, in acid catalysis, and at a temperature ranging from 50° to 120°C, of 2 to 10 mol of glycidol per mole of either alcohol containing 10 to 14 carbon atoms or of alpha-diol containing 10 to 14 carbon atoms; and

(C) the poly(hydroxypropyl ether) compounds prepared by polyaddition of glycerol monochlorohydrin to a polyhydroxylated organic compound in the presence of a strong base, with removal of water, by distillation, as said water is formed.

5. A composition according to claim 4, wherein:

a) R denotes a C₁0 -C₁4 alkyl radical or a mixture of C₁0 -₁4 alkyl radicals, and n is a whole or decimal number from 3 to 6;

b) R denotes a group of said formula (II) and n denotes a whole or decimal number from 1.5 to 4;

c) R denotes a group of said formula (III),

wherein the aliphatic chains denote alkyl chains which can contain from 1 to 6 ether groups, thioether groups, hydroxymethylene groups, and mixtures of any of said groups; and

(B) the poly(hydroxypropyl ether) compounds prepared by condensation, in acid catalysis, and at a temperature ranging from 50° to 120°C, of 2.5 to 6 mol of glycidol per mole of either alcohol containing 10 to 14 carbon atoms or of alpha-diol containing 10 to 14 carbon atoms.

6. A composition according to claim 4, wherein said at least one non-ionic poly(hydroxypropyl ether) surfactant is selected from the following compounds: ##STR6## in which formula (V), R₁ denotes a mixture of C₁0 H₂1 and C₁2 H₂5 alkyl radicals,

2i) the compounds prepared by condensation, in alkaline catalysis, of 3.5 mol of glycidol with an alpha-diol having 12 carbon atoms,

3i) the compounds of formula (VI):

R₂ --CONH--CH₂ --CH₂ --O--CH₂ CH₂ --O--(--CH₂ --CHOH--CH₂ --O--)₃.5 --H (VI)

in which R₂ denotes a mixture of radicals comprising the following alkyl and alkenyl radicals: C₁1 H₂3, C₁3 H₂7, the radicals derived from coconut fatty acids and the radical derived from oleic acid and

4i) the compounds prepared by condensation of 3.5 mol of glycidol with a mixture of C₁1 -C₁4 alpha-diols.

7. A composition according to claim 4, wherein said at least one non-ionic poly(hydroxypropyl ether) surfactant is a dodecanediol polyglycerolated with 3.5 mol of glycerol.

8. A composition according to claim 1, wherein said composition is a composition for oral hygiene.

9. A composition according to claim 8, wherein said composition for oral hygiene is a dentifrice.

10. A composition according to claim 8, wherein said composition for oral hygiene is a toothpaste or tooth gel.

11. A composition according to claim 8, wherein said composition for oral hygiene is a chewing gum.

12. A composition comprising, in an aqueous vehicle, an abrasive system containing at least one alkali metal bicarbonate and a surfactant system, wherein said surfactant system consists of at least one nonionic poly(hydroxypropyl ether) surfactant.